Preliminary and ongoing French multicenter prospective naturalistic study of adverse events of antipsychotic treatment in naive children and adolescents
© Menard et al.; licensee BioMed Central Ltd. 2014
Received: 22 February 2014
Accepted: 2 June 2014
Published: 13 June 2014
The prescription of antipsychotics (AP), and especially second generation AP, is increasing worldwide in the pediatric population. Most prescriptions are off-label and despite the identification of frequent and potentially severe adverse events (AE), there are only a few guidelines for the safety management. France is one of the countries with no official safety guidelines.
Psychotropic drug-naive adolescents (13–18 years), hospitalized for an acute psychotic episode and treated with a second-generation antipsychotic were consecutively included in a prospective cohort study. Patients were assessed for their AE at baseline, 2, 6 and 12 weeks after the introduction of drug.
The majority of patients was treated with risperidone (n = 13), 2 with aripiprazole. The principal findings are: (1) A high incidence of neuromuscular AE: 8/15 muscle weakness, 8/15 extrapyramidal syndrome, 6/15 akathisia, 3/15 oro-facial acute dystonia; (2) Severe catatonia symptoms in 2 patients despite a low to moderate treatment dose, requiring transfer in intensive care unit for one; (3) Weight gain and significant increase of the BMI for all 13 patients who had a 12 weeks follow-up.
All adolescents experienced AE, with significant weight gain being observed in all patients who completed the 12-week follow-up. The fact that our patient population was first episode drug naïve may partially explain this observation. Despite the limitation due to the small sample size of this prospective short-term study, such findings are important to report and warrant further research.
Clinical and research implication
Because of the lack of naturalistic follow up studies of antipsychotic treatments in AP-naive children and adolescents and the absence of safety guidelines for the pediatric population in France, we decided to continue our research at a national level. We therefore started a prospective, naturalistic and multicenter study funded by the French National Agency for Medicines and Health Products Safety (ANSM). Study purpose is to evaluate the incidence of adverse events related to antipsychotic drugs in AP-naive children and adolescents. In addition, we aim to provide further evidence for the necessity of national safety guidelines for AP prescription in the pediatric population.
KeywordsAdverse drug events Antipsychotics Therapeutic drug monitoring Drug-naïve population Child psychiatry Pediatrics
The prescription of psychotropics has increased in the pediatric population all over the world since about 15 years. This increase is widely varying depending on the country and molecules, ranging from 1.5- to 5-times in many European countries and the United States [1, 2]. In France the frequency of annual psychotropic prescriptions in children and adolescents is about 2.2% . The increase in antipsychotic (AP) use is explained by a dramatic increase in atypical or second-generation AP (SGA) use, while typical or first-generation AP (FGA) prescriptions decreased . SGA have a comparable efficiency to FGA with better neuromuscular safety . Many AP medications in the pediatric population are prescribed off-label, especially in very young children [5, 6]. Prescriptions are therefore frequently unsupported by rigorous scientific evidence. SGA drugs are actually widely used to treat many psychiatric disorders such as schizophrenia, bipolar, autistic spectrum, attention deficit hyperactivity or behavior disorders in the pediatric population [7–9]. However, the pediatric literature data show several adverse events (AE) in children and adolescents treated with AP [10–14]: muscular (muscle weakness, extrapyramidal syndrome, akathisia, dystonia, dyskinesia, catatonia), metabolic (weight gain, obesity, dyslipidemia, hyperglycemia, diabetes, insulin resistance, hypertriglyceridemia, hypercholesterolemia) and endocrine AE (hyperprolactinemia, vitamin D deficiency). Children treated with SGA are more likely than adults to experience AE. Woods et al.  studied more than 4 million prescriptions of olanzapine. They observed that the relative risk of sedation, weight gain, dystonia and tardive dyskinesia is 2 to 5 times greater in children or adolescents than in adults. Additionally, only few prospective studies examine antipsychotic adverse events in naive pediatric populations [16–18]. Several European and American authors are worried about long-term effects of antipsychotic medication on children’s health and recommend more safety guidelines and management of adverse events [19–26]. In fact, there are currently few guidelines for the management of adverse events in youth treated by antipsychotics [27–29]. On the European level, the lack of official guidelines for standardized follow-ups in the pediatric population is surprising given the probably higher relative risk of AE in this population. Furthermore, the incidence of AE in a drug-naive population is less well documented, as the typical study populations consist of pediatric patients who have already been exposed to an antipsychotic drug [30, 31]. In France, since 2007 only two second-generation antipsychotics have been granted market authorization: risperidone for severe behavioral disorders from 5 years of age; and aripiprazole for schizophrenia from the age of 15 years and recently for maniac episodes associated with bipolar I disorder from the age of 13. The frequency of antipsychotic off-label prescriptions is as high as 69% in French university pediatric hospitals . In March 2010, the French National Agency for Medicines and Health Products Safety (Agence nationale de sécurité du médicament et des produits de santé, ANSM) recommended cardiometabolic monitoring for all adult subjects treated with psychotropic drugs. There is no official recommendation for the safety monitoring in the pediatric population. This is paradoxical, since this population is at high risk of adverse events. In addition, adverse events during AP use in children are often poorly and insufficiently monitored in France in general practice.
In our own clinical experience, based on a university inpatient unit specifically aimed to treat young adolescents with a first psychotic episode, we have observed that adverse events (AE) such as weight gain, acute dystonia and catatonia were very common in these patients treated for the first time with SGA. We therefore undertook a naturalistic prospective cohort study in the University Children and Adolescent Psychiatric Department of Nice, France, in order to evaluate the incidence of AE related to SGA and we present the main results observed in our clinical population. This psychiatric department is the only inpatient adolescent psychiatric facility serving the one million and a half inhabitants of the French department of the Alpes-Maritimes. Inpatient psychotropic naive adolescents presenting a first acute psychotic episode and treated with a SGA were consecutively included in the study over a 12-month period from July 2009 to July 2010. Each patient was followed for 12 weeks.
We observed a high incidence of neuromuscular AE during the follow-up, leading to the discontinuation of AP treatment (risperidone) in 3 patients (catatonia 2/3, acute oro-facial dystonia 1/3). Muscle weakness was reported in 8/15 subjects, extrapyramidal syndrome in 8/15, akathisia in 6/15 and acute oro-facial dystonia in 3/15.
Severe catatonia symptoms were observed in 2 patients with paranoid schizophrenia at the 4th and 7th day of treatment while receiving a low to moderate dose of risperidone (1.5 and 2 mg respectively). Both patients presented stupor, mutism, staring, catalepsy and rigidity. In addition, verbigeration and withdrawal with refusal to eat and drink was a clinical feature in the first patient, and echolalia and impulsivity in the second one. Patients did not have fever or dysfunctions of the autonomic nervous system. They presented high scores on the Bush Francis Catatonia Rating Scale (17 and 12 respectively). SGA was immediately stopped and patients received clonazepam at dose 0.05 mg/kg/d. The first patient had to be transferred to the intensive care unit for hypoglycemia and dehydration in order to receive intravenous treatment.
One patient presented acute oro-facial dystonia. AP treatment was stopped and the patient received anticholinergic medication (one dose of intramuscular tropatepine 10 mg).
Moderate akathisia was present in 6 patients, sometimes starting as early as 2 weeks of SGA treatment. Severity was evaluated using the Extrapyramidal Symptom Rating Scale (ESRS).
For all patients - with the exception for one patient who developed catatonia - creatine phosphokinase was normal during follow up despite of a significant increase (p = 0.03, Wilcoxon test). No correlation was detected between this increase and neuromuscular AE (muscle weakness, extrapyramidal syndrome, akathisia).
The 12 patients who completed the 12 weeks follow-up presented a significant weight gain with 51.1 ± 8.5 kg at W0 and 59.0 ± 11.2 kg at W12 (p = 0.002, Wilcoxon test). The BMI increased significantly from 19.0 ± 2.5 at W0 to 21.7 ± 3.5 at W12 (p = 0.002). The observed weight gain of about 8 kg during 12 weeks is higher than in two other pediatric studies of comparable duration (3,9 et 5,3 kg for risperidone [40, 30]; 4,4 kg for aripiprazole ; this might be explained by the small subject number or dose differences in our study.
No abnormalities were observed for the other monitored parameters, including lipid values.
In summary, we observed in our study many and serious adverse events despite the small sample size of 15 subjects. The particularity of this study is that all patients presented a first psychotic episode and had never been exposed to antipsychotic and/or other psychotropic medications before, which might partially explain this observation. For all these reasons and because of the lack of naturalistic follow-up studies of antipsychotic treatments in naive children and adolescents in France, we wanted to continue studying at the national level.
A multicenter prospective naturalistic study in antipsychotic naive children (ETAPE Study)
In the pediatric population, the use of antipsychotic drugs has been continously increasing over the last decade. In France, prescriptions are frequently off-label and starting more and more in young children. Adverse events are often not optimally monitored and without systematic follow-up. In addition, the lack of studies in children also leads to a safety concern.
The data of our preliminary study underline a high prevalence of neuromuscular AE in fifteen psychotropic drug naive inpatient adolescents treated with SGA for a first psychotic episode. We therefore started a multicenter prospective and naturalistic study to evaluate AP adverse events in naive children and adolescents in France. The results of ETAPE’s study will have a major impact in terms of public mental health services in our country and must help to develop official recommendations for antipsychotic treatment and its safety monitoring in the pediatric population.
Implications and contribution
Beyond the available literature, more research is urgently needed about adverse events of antipsychotics in the pediatric population in order to develop official recommendations. However, enough is known to emphasize the necessity of thorough and systematic monitoring of AE in this vulnerable population. Furthermore, in the light of the growing trend to prescribe these drugs to children and adolescents, practitioners need to be aware of the necessity of optimal safety management.
The study was approved by Lenval Children's Hospital Scientific Committee. Written informed consent was obtained from the patients and their parents.
The authors would like to thank the patients and their parents for participation in these studies. The ETAPE study is supported by the French National Agency for Medicines and Health Products Safety (Agence Nationale de Sécurité du Medicament et des produits de santé, ANSM).
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